Date published: 2025-10-17

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Stachybotrylactam (CAS 163391-76-2)

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Application:
Stachybotrylactam is a potentially useful mycotoxin isolated from Stachybotrys sp.
CAS Number:
163391-76-2
Purity:
>95%
Molecular Weight:
385.5
Molecular Formula:
C23H31NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Stachybotrylactam is a unique macrocyclic lactam isolated from the fungus Stachybotrys chartarum, known for its presence in damp, water-damaged buildings and its association with a variety of environmental toxins. The compound′s structure features a 12-membered ring lactam, a rare motif that provides interesting biological and chemical properties for scientific study. In research, stachybotrylactam has been studied for its intriguing ability to modulate biochemical pathways without being directly linked to therapeutic uses. Its mechanism of action is primarily related to its interaction with cellular proteins, particularly those involved in transcription and the regulation of gene expression. Due to its macrocyclic structure, stachybotrylactam can fit into and block protein domains, thereby inhibiting protein-protein interactions that are crucial for the normal function of certain cellular processes. One of the key focuses of research on stachybotrylactam has been its role in affecting the activity of transcription factors and other nuclear proteins. By altering the behavior of these proteins, stachybotrylactam helps researchers understand the complex dynamics of cellular regulation and the importance of structural conformation in these processes. Moreover, stachybotrylactam serves as a chemical probe in the study of enzyme inhibition. Its ability to bind and possibly inhibit certain enzymes offers insights into the modulation of enzymatic activity, providing a clearer view of how specific enzymes contribute to cell metabolism and signaling.


Stachybotrylactam (CAS 163391-76-2) References

  1. Enantioselective total synthesis and structure revision of spirodihydrobenzofuranlactam 1. Total synthesis of stachybotrylactam.  |  Kende, AS., et al. 2003. Org Lett. 5: 1785-8. PMID: 12735777
  2. Total synthesis and structure revision of stachybotrys spirolactams.  |  Deng, WP., et al. 2003. J Org Chem. 68: 7422-7. PMID: 12968895
  3. Three new phenylspirodrimane derivatives with inhibitory effect towards potassium channel Kv1.3 from the fungus Stachybotrys chartarum.  |  Feng, JM., et al. 2019. J Asian Nat Prod Res. 21: 887-894. PMID: 30614271
  4. Toxin Production by Stachybotrys chartarum Genotype S on Different Culture Media.  |  Ulrich, S. and Schäfer, C. 2020. J Fungi (Basel). 6: PMID: 32887224
  5. Occurrence of type A, B and D trichothecenes, zearalenone and stachybotrylactam in straw.  |  Ulrich, S., et al. 2021. Arch Anim Nutr. 75: 105-120. PMID: 33615927
  6. In vitro screening of 65 mycotoxins for insecticidal potential.  |  Boguś, MI., et al. 2021. PLoS One. 16: e0248772. PMID: 33735295
  7. The Occurrence and Co-Occurrence of Regulated, Emerging, and Masked Mycotoxins in Rice Bran and Maize from Southeast Asia.  |  Siri-Anusornsak, W., et al. 2022. Toxins (Basel). 14: PMID: 36006229
  8. New Phenylspirodrimanes from the Sponge-Associated Fungus Stachybotrys chartarum MUT 3308.  |  Dayras, M., et al. 2023. Mar Drugs. 21: PMID: 36976184
  9. A Chemically Defined Medium That Supports Mycotoxin Production by Stachybotrys chartarum Enabled Analysis of the Impact of Nitrogen and Carbon Sources on the Biosynthesis of Macrocyclic Trichothecenes and Stachybotrylactam.  |  Tribelhorn, K., et al. 2023. Appl Environ Microbiol. 89: e0016323. PMID: 37338364

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Stachybotrylactam, 500 µg

sc-202345
500 µg
$350.00